retrosynthesis
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Etymology
[edit]Noun
[edit]retrosynthesis (countable and uncountable, plural retrosyntheses)
- (organic chemistry) The prediction of precursors (intermediates and reactants), given the products of a synthesis reaction.
- 1983, Francis A. Carey, Richard J. Sundberg, Advanced Organic Chemistry: Reactions and synthesis, Plenum Press, page 578,
- The retrosyntheses shown in Scheme 11.11 correspond to the syntheses in Schemes 11.12 and 11.13.
- 1991, Australian Journal of Chemistry, Volume 44, CSIRO, page 1294:
- The retrosyntheses shown in Scheme 2 lead directly to acetylene-type retrons (14)-(16) (path a) or implicate the use of Dewar o-xylylene (17) (path b) and the smaller retrons (18)-(20); the latter path was the route we elected to pursue (Scheme 3).
- 2007, Helmut Cölfen, “Bio-inspired Mineralization Using Hydrophilic Polymers”, in Kensuke Naka, editor, Biomineralization II: Mineralization Using Synthetic Polymers and Templates, Springer, page 25:
- For example, the above mentioned retrosynthesis of nacre [132] is as much bio-inspired as is the crystallization in presence of hydrophilic polymers [44], although in the first case, the original biomineral structure is reproduced, whereas in the latter case, no biomineral is reproduced but complex crystal morphologies are obtained.
- 1983, Francis A. Carey, Richard J. Sundberg, Advanced Organic Chemistry: Reactions and synthesis, Plenum Press, page 578,
Synonyms
[edit]- (prediction of precursors): retrosynthetic analysis
Derived terms
[edit]Related terms
[edit]Translations
[edit]prediction of precursors in a synthesis reaction
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See also
[edit]Further reading
[edit]Retrosynthetic analysis on Wikipedia.Wikipedia
Elias James Corey on Wikipedia.Wikipedia
Organic synthesis on Wikipedia.Wikipedia
Total synthesis on Wikipedia.Wikipedia